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287 items found for "Duc Tin Tran"
- Free-Energy Simulations Support a Lipophilic Binding Route for Melatonin Receptors
ligand access to the orthosteric binding site of MT1 and MT2 receptors through a lateral channel between transmembrane
- Phenylalanine 193 in Extracellular Loop 2 of the β 2-Adrenergic Receptor Coordinates β-Arrestin ...
β 2-Adrenergic Receptor Coordinates β -Arrestin Interaction G protein-coupled receptors (GPCRs) transduce Using bioluminescence resonance energy transfer -based biosensors, second messenger assays, and biochemical undescribed role for the extracellular loops of the receptor and the extracellular pocket formed by transmembrane
- Exendin-4 Attenuates Remodeling in the Remote Myocardium of Rats After an Acute Myocardial ...
reactive oxygen species (ROS) and inflammatory cytokines, as well as protein levels of Wnt1, phospho-Akt, transforming Β-catenin activation and nuclear translocation are associated with increased synthesis of inflammatory cytokines and transforming growth factor β-1 (TGF-β1). TGF-β1 stimulates the phosphorylation of Smad-3 and subsequent nuclear translocation to activate the transcription of collage 1/III and α-smooth muscle actin (α-SMA).
- Odorant G protein-coupled receptors as potential therapeutic targets for adult diffuse gliomas ...
In addition to transcriptomic analysis, mutational profiles revealed that somatic mutations in OR genes Based on this systematic analysis and review of the genomic and transcriptomic profiles of ORs in glioma
- Neuronal Gα subunits required for the control of response to polystyrene nanoparticles in the ...
In nematodes, exposure to PS-NPs (1-100 μg/L) significantly altered transcriptional expressions of some Therefore, neuronal Gα proteins of GOA-1, GSA-1, and GPA-10 functioned to transduce signals of multiple
- Disentangling bias between G q, GRK2, and arrestin3 recruitment to the M 3 muscarinic acetylcholine
G protein-coupled receptors (GPCRs) transmit extracellular signals to the inside by activation of intracellular
- GPCRS: AN ODYSSEY FROM STRUCTURE, SIGNALING AND REGULATION TO THERAPEUTICS
challenges in the study of GPCR action in multiple systems, but also offers exciting opportunities in the translational